United States · FDA National Drug Code directory
Minocycline Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63629-9210_b88e6ee2-70d3-4d6a-bdff-1cafbb2b9daf
- Product NDC
- 63629-9210
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Minocycline Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160930
- Source listing expiry
- 20261231
Source-listed ingredients
- MINOCYCLINE HYDROCHLORIDE — 135 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9210-1) · 63629-9210-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →